A. Kongchanagul, P. Masrinoul, C. Boonarkart, O. Suptawiwat, P. Auewarakul
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引用次数: 0
摘要
血凝素(HA)是流感病毒表面的主要包膜糖蛋白和抗原。这种糖蛋白由球状的头部和柄部组成。流感病毒 HA 头部的免疫优势表位变化很大,而柄区则是保守的。HA 头部的变异导致抗原漂移,因此需要每年更新疫苗株。诱导针对柄结构域的抗体被认为是一种具有广泛保护作用的流感疫苗策略。有研究表明,连续暴露于具有高度不同的 HA 头部但茎部保持不变的流感病毒株,可诱导对低免疫原性茎部结构域的抗体。在这里,我们使用进化过程中相隔几十年的老流感疫苗株来测试这种方法。将 A/波多黎各/8/1934、A/苏联/92/1977 和 A/泰国/102/2009(H1N1)流感全病毒灭活疫苗依次免疫给 BALB/c 小鼠,与使用单一毒株(A/泰国/102/2009(H1N1))免疫进行比较。顺序免疫的小鼠产生了更高水平的柄结构域结合抗体。这表明,使用旧疫苗株进行顺序免疫可能是诱导保守柄结构域抗体的一种可行方法。
Antibody Response to Influenza Hemagglutinin Conserved Stalk Domain after Sequential Immunization with Old Vaccine Strains
Hemagglutinin (HA) is the major envelope glycoprotein and antigen on the surface of influenza virions. The glycoprotein comprises a globular head and a stalk region. While immunodominant epitopes on influenza HA head are highly variable, the stalk domain is conserved. The variability of the HA head causes the antigenic drift that made the requirement of annual update of vaccine strains. Induction of antibody against the stalk domain has been proposed as an approach for a broadly protective influenza vaccine strategy. Sequential exposure to influenza strains with highly diverse HA heads but conserved stalks have been shown to induce antibody to the low immunogenic stalk domain. Here, we tested this approach by using old influenza vaccine strains that are decades apart in evolution. Inactivated whole virion vaccine of influenza A/Puerto Rico/8/1934, A/USSR/92/1977, and A/Thailand/102/2009 (H1N1) was sequentially immunized into BALB/c mice in comparison to immunization using single strain (A/Thailand/102/2009 (H1N1)). The sequentially immunized mice developed higher levels of binding antibody to the stalk domain. These suggested that using old vaccine strains in sequential vaccination may be a possible approach to induce antibody to the conserved stalk domain.